Canonical Allele Identifier: CA2668196871

Gene: CLRN1

Linked Data

• gnomAD v4: 3-150926684-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150926684C>A , CM000665.2:g.150926684C>A	GRCh38
NC_000003.11:g.150644471C>A , CM000665.1:g.150644471C>A	GRCh37
NC_000003.10:g.152127161C>A	NCBI36
NG_009168.1:g.51316G>T , LRG_700:g.51316G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000327047.6:c.*1252G>T MANE Select	ENSP00000322280.1:n.*1252G>T
ENST00000295911.6:c.*168G>T	ENSP00000295911.2:n.*168G>T
ENST00000327047.5:c.*1252G>T	ENSP00000322280.1:n.*1252G>T
ENST00000562308.5:c.104+14898G>T
ENST00000565169.1:c.162+14898G>T
ENST00000569170.5:c.162+14898G>T
NM_001195794.1:c.*1252G>T , LRG_700t1:c.*1252G>T	NP_001182723.1:n.*1252G>T
NM_001256819.1:c.*1565G>T	NP_001243748.1:n.*1565G>T
NM_052995.2:c.*168G>T , LRG_700t2:c.*168G>T	NP_443721.1:n.*168G>T
NM_174878.2:c.*1252G>T	NP_777367.1:n.*1252G>T
NR_046380.2:n.2432G>T
XR_924167.1:n.2263G>T
NM_001256819.2:c.*1565G>T	NP_001243748.1:n.*1565G>T
NM_174878.3:c.*1252G>T MANE Select	NP_777367.1:n.*1252G>T
NR_046380.3:n.2160G>T